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Chemical Science
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October 3, 2017
Next-generation disulfide stapling: reduction and functional re-bridging all in one
Maximillian T W Lee, Antoine Maruani, James R Baker, et al.
Chemical Science
|
April 29, 2017
Enabling the controlled assembly of antibody conjugates with a loading of two modules without antibody engineering
Maximillian T W Lee, Antoine Maruani, Daniel A Richards, et al.
Chemical Communications (Cambridge, England)
|
November 21, 2014
A mild TCEP-based para-azidobenzyl cleavage strategy to transform reversible cysteine thiol labelling reagents into irreversible conjugates
Antoine Maruani, Shamim Alom, Pierre Canavelli, et al.
RSC Advances
|
May 2, 2022
Cysteine specific bioconjugation with benzyl isothiocyanates
László Petri, Péter A Szijj, Ádám Kelemen, et al.
RSC Chemical Biology
|
February 23, 2026
Enabling the synthesis of multi-payload thio-antibody conjugates through the use of pyridazinediones, <i>p</i>-anisidine derivatives and various click chemistries
Clíona McMahon, Christophe J Queval, Ioanna A Thanasi, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 5) with videos related to
Sort By:
Page
of 1
Chemical Science
|
October 3, 2017
Next-generation disulfide stapling: reduction and functional re-bridging all in one
Maximillian T W Lee, Antoine Maruani, James R Baker, et al.
Chemical Science
|
April 29, 2017
Enabling the controlled assembly of antibody conjugates with a loading of two modules without antibody engineering
Maximillian T W Lee, Antoine Maruani, Daniel A Richards, et al.
Chemical Communications (Cambridge, England)
|
November 21, 2014
A mild TCEP-based para-azidobenzyl cleavage strategy to transform reversible cysteine thiol labelling reagents into irreversible conjugates
Antoine Maruani, Shamim Alom, Pierre Canavelli, et al.
RSC Advances
|
May 2, 2022
Cysteine specific bioconjugation with benzyl isothiocyanates
László Petri, Péter A Szijj, Ádám Kelemen, et al.
RSC Chemical Biology
|
February 23, 2026
Enabling the synthesis of multi-payload thio-antibody conjugates through the use of pyridazinediones, <i>p</i>-anisidine derivatives and various click chemistries
Clíona McMahon, Christophe J Queval, Ioanna A Thanasi, et al.
Page
of 1